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nsv5472444

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,284

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 347 SVs from 48 studies. See in: genome view    
Submitted genomic111,081,251-111,111,534Question Mark
Overlapping variant regions from other studies: 349 SVs from 48 studies. See in: genome view    
Remapped(Score: Good):110,416,949-110,447,233Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5472444Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5111,081,251111,111,534
nsv5472444RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5110,416,949110,447,233

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973659duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973659Submitted genomicNC_000005.10:g.111
081251_111111534du
p
GRCh38 (hg38)NC_000005.10Chr5111,081,251111,111,534
nssv16973659RemappedGoodNC_000005.9:g.1104
16949_110447233dup
GRCh37.p13First PassNC_000005.9Chr5110,416,949110,447,233

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16973659<0.00146404
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